HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005601Generated: October 30, 2026
Sodium borohydride → HCID 18791562, compound
https://huagongshe.com/reaction/1005601
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18791297 | HCID 18791297 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18791562 | HCID 18791562 | 103.4% |
Reaction Steps
To a solution of 4-[2-[(3-tert-butoxycarbonylaminoprop-1-yl)oxy]benzoyl]amino-3-methoxy-N-methyl-N-[2-[5-(4-oxopiperidin-1-yl)carbonylpent-1-yl]oxy-4-methylphenyl]benzamide (192 mg) in methanol (5 ml) was added sodium borohydride (19 mg) at ambient temperature and the mixture was stirred at the same temperate for 1 hour. The reaction was quenched with 0.5N hydrochloric acid (10 ml) and the mixture was extracted with chloroform (15 ml×3). The organic layer was washed with aqueous sodium hydrogen carbonate and brine, and the solution was dried over magnesium sulfate. The solvent was evaporated in vacuo to give 4-[2-[(3-tert-butoxycarbonylaminoprop-1-yl)oxy]benzoyl]amino-3-methoxy-N-methyl-N-[2-[5-(4-hydroxypiperidin-1-yl)carbonylpent-1-yl]oxy-4-methylphenyl]benzamide (199 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06054457 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-ff86be55fead4fc1bbe189cb11cfceb7 |
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| Source note | uspto-grants-2000_04 |
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